DISEASES

Disease-gene associations mined from literature

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Human genes for hyperprolactinemia

Hyperprolactinemia [DOID:12700]

An acquired metabolic disease that has_material_basis_in the presence of abnormally-high levels of prolactin in the blood.

Synonyms:  hyperprolactinemia,  DOID:12700,  hyperprolactinemias,  Chiari-Frommel syndrome,  hyperprolactinaemia ...

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.